GTF2I - general transcription factor IIi Gene

Also Known as WBS; DIWS; SPIN; IB291; BAP135; BTKAP1; TFII-I; WBSCR6; GTFII-I

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 2969

About GTF2I

Cytogenetic location: 7q11.23 Genomic coordinates (GRCh38): 7:74,657,718-74,760,692 (from NCBI)

This gene has 24 transcripts (splice variants), 130 orthologues, 18 paralogues and is associated with 1 phenotype. Ubiquitous expression in brain (RPKM 105.1), thyroid (RPKM 95.5) and 25 other tissues.

Summary

This gene encodes a phosphoprotein containing six characteristic repeat motifs. The encoded protein binds to the initiator element (Inr) and E-box element in promoters and functions as a regulator of transcription. This locus, along with several Other neighboring genes, is deleted in Williams-Beuren syndrome. There are many closely related genes and pseudogenes for this gene on chromosome 7. This gene also has pseudogenes on chromosomes 9, 13, and 21. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Jul 2013]

GTF2I Products (6)

mRNA Protein Name
NM_001163636.3 NP_001157108.1 general transcription factor II-I isoform 5
NM_001280800.2 NP_001267729.1 general transcription factor II-I isoform 6
NM_001518.5 NP_001509.3 general transcription factor II-I isoform 4
NM_032999.4 NP_127492.1 general transcription factor II-I isoform 1
NM_033000.4 NP_127493.1 general transcription factor II-I isoform 2
NM_033001.4 NP_127494.1 general transcription factor II-I isoform 3
Molecular Function GO Annotation Evidence References Source
enables DNA-binding transcription activator activity, RNA polymerase II-specific IDA
IDA: Inferred from direct assay
9334314 GOA
enables RNA polymerase II-specific DNA-binding transcription factor binding IPI
IPI: Inferred from physical interaction
9334314 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
9012831 GOA
Biological Process GO Annotation Evidence References Source
acts upstream of or within negative regulation of angiogenesis IDA
IDA: Inferred from direct assay
19242469 GOA
involved in positive regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
9334314 GOA
Cellular Component GO Annotation Evidence References Source
located in nucleus IDA
IDA: Inferred from direct assay
19242469 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

GTF2I Protein Structure

GTF2I

GTF2I: GTF2I-like repeat (112 - 187)

GTF2I

GTF2I: GTF2I-like repeat (361 - 435)

GTF2I

GTF2I: GTF2I-like repeat (466 - 541)

GTF2I

GTF2I: GTF2I-like repeat (571 - 646)

GTF2I

GTF2I: GTF2I-like repeat (733 - 808)

GTF2I

GTF2I: GTF2I-like repeat (868 - 943)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 998 a.a.
Protein Preferred Names Protein Names

general transcription factor II-I

  • BTK-associated protein, 135kD

GTF2I Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
GTF2I P78347 BRCA1 Homo sapiens P38398 21407215
Intra
GTF2I P78347 BRCA1 Homo sapiens P38398 21407215
Intra
GTF2I P78347 BTK Homo sapiens Q06187 9012831
Cross: Cross-species interaction Intra: Intraspecies interaction

GTF2I Antibodies

Cat. No. Product Name Application Reactivity
HY-P83523 General Transcription Factor II I Antibody (YA3268) WB, IHC-P, ICC/IF Human, Mouse, Rat
HY-P83523A General Transcription Factor II I Antibody (YA3268)(PBS only) WB, IHC-F, IHC-P, ICC/IF Human

Related Diseases

Diseases Alias
Williams-Beuren Syndrome
  • Williams Syndrome

  • WBS

  • Wms

  • Deletion 7q11.23

  • Monosomy 7q11.23

  • Chromosome 7q11.23 Deletion Syndrome, 1.5- To 1.8-Mb

  • Fanconi Schlesinger Syndrome

  • Beuren Syndrome

  • Elfin Facies Syndrome

  • Elfin Facies With Hypercalcemia

  • Hypercalcemia-Supravalvar Aortic Stenosis

  • Ws

Supravalvular Aortic Stenosis
  • SVAS

  • Supravalvar Aortic Stenosis

  • Supravalvar Aortic Stenosis, Eisenberg Type

  • Aortic Supravalvular Stenosis

  • Aortic Stenosis, Supravalvular

  • Supra-Valvular Aortic Stenosis

  • Stenosis, Aortic Supravalvular

  • Stenosis, Supravalvular Aortic

  • Supravalvular Stenosis, Aortic

  • Aortic Stenosis Supravalvular

Thymoma
  • Primary Thymic Epithelial Neoplasm

  • Primary Thymic Epithelial Tumor

  • Thymus Neoplasms

Williams-Beuren Region Duplication Syndrome
  • 7q11.23 Duplication Syndrome

  • 7q11.23 Microduplication Syndrome

  • Chromosome 7q11.23 Duplication Syndrome

  • Wbs Duplication Syndrome

  • Somerville-Van Der Aa Syndrome

  • Dup(7)(Q11.23)

  • Trisomy 7q11.23

  • William-Beuren Region Duplication Syndrome

  • Chromosome 7q11.23 Duplication

Dyslexia
Immune System Organ Benign Neoplasm
Thymus Lipoma
  • Thymolipoma

Mediastinum Sarcoma
  • Sarcoma Of Mediastinum

Chromosomal Deletion Syndrome
Thymic Carcinoma
  • Malignant Thymoma

  • Thymoma, Malignant

Intellectual Developmental Disorder, X-Linked 108
  • MRX108

  • X-Linked Intellectual Developmental Disorder 108

  • Mental Retardation, X-Linked 108

  • Mental Retardation, X-Linked, Type 108

Thymus Gland Disease
  • Disease Of Thymus Gland

Thymus Cancer
  • Thymic Neoplasm

  • Thymic Tumor

  • Thymus Neoplasm

  • Thymus Neoplasms

  • Malignant Neoplasm Of Thymus

  • Neoplasm Of Thymus

  • Thymic Neoplasms

  • Thymoma, Familial

  • Thymic Carcinoma

  • Thymoma, Type C

  • Cancer Of Thymus

  • Malignant Tumour Of Thymus

  • Primary Malignant Neoplasm Of Thymus

  • Thymic Glandular Cancer

  • Thymus Gland Cancer

Chromosomal Disease
  • Chromosomal Disorders

  • Congenital Chromosomal Disease

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus GTF2I MGD MGI:1202722
Rattus norvegicus GTF2I RGD RGD:727961
Bos taurus GTF2I VGNC VGNC:29699
Macaca mulatta GTF2I VGNC VGNC:73313
Felis catus GTF2I VGNC VGNC:67501
Canis familiaris GTF2I VGNC VGNC:54032
Others GTF2I NCBI